16 results
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36ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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KIT FLU A+B 30 TEST HOSPITAL VERITOR
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·December 9, 2021
KIT FLU A+B 30 TEST HOSPITAL VERITOR
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·December 9, 2021
KIT FLU A+B 30 TEST HOSPITAL VERITOR
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·December 9, 2021
KIT FLU A+B 30 TEST HOSPITAL VERITOR
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·December 9, 2021
KIT FLU A+B 30 TEST HOSPITAL VERITOR
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·December 9, 2021
BD KIT FLU A+B 30 TEST PHYSICIAN VERITOR
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code PSZ·December 6, 2021
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 11, 2013
ONE TOUCH ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·May 22, 2008
FINE NEEDLE ELECTRODE
FDA Adverse Event
Malfunction
·COVIDIEN VALLEYLAB·Product code GEI·April 8, 2011
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWS·February 22, 2024
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code FMI·January 24, 2019
BD VERITOR¿ PLUS ANALYZER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code GTY·December 16, 2021
BD VERITOR¿ PLUS ANALYZER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code GTY·December 16, 2021
BD VERITOR¿ PLUS ANALYZER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code GTY·December 16, 2021
BD VERITOR¿ PLUS ANALYZER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code GTY·December 16, 2021
BD VERITOR¿ PLUS ANALYZER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code GTY·December 16, 2021